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Design of enediyne prodrugs.

M. E. Maier, Synlett, 1995, 13.

Key Words:
GENERAL STRATEGIES FOR GENERATING REACTIVE ENEDIYNES/FACTORS THAT INFLUENCE THE REACTIVITY OF ENEDIYNES/1,5-DIYNES AS PRODRUGS/ENEDIYNE PRODRUGS WITH A BRIDGEHEAD DOUBLE BOND/ENEDIYNE PRODRUGS WITH AN EPOXIDE AS BLOCKING DEVICE/OTHER ENEDIYNE-CONTAINING PRODRUGS/CONCLUSION/CALICHEAMICIN-ESPERAMICIN ANALOGS/CYCLIC CONJUGATED ENEDIYNES/DNA-CLEAVING MOLECULES/DYNEMICIN-A/ANTITUMOR ANTIBIOTICS/CHEMICAL SYNTHESIS/DYOTROPIC REARRANGEMENTS/ANTICANCER ANTIBIOTICS/BIRADICAL FORMATION/TRIGGERING DEVICES



Synthesis of medium-sized rings by the ring-closing metathesis reaction.

M. E. Maier, Angew. Chem., Int. Ed. Engl., 2000, 39, 2073.

Key Words:
cyclizations/medium-sized rings/metathesis/synthetic methods/OLEFIN METATHESIS/EPOTHILONE-A/IMIDAZOLIN-2-YLIDENE LIGANDS/NORTHERN-HEMISPHERE/ORGANIC-SYNTHESIS/BICYCLIC LACTAMS/10-MEMBERED RING/ROSEOPHILIN/CONSTRUCTION/COMPLEXES



Design and synthesis of dynemicin analogs.

M. E. Maier, F. Bosse, A. J. Niestroj, Eur. J. Org. Chem., 1999, 1.

Key Words:
dynemicin/enediynes/antitumor agents/antibiotics/cross-coupling/ANTITUMOR ANTIBIOTIC DYNEMICIN/WIDE STRUCTURAL VARIABILITY/ARYL CARBAMATE MOIETIES/CHEMICAL SYNTHESIS/MOLECULAR DESIGN/DNA-CLEAVAGE/CYCLIC ENEDIYNES/BIOLOGICAL PROPERTIES/BIOACTIVE ANALOGS/METHIDE FORMATION